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1.
《Applied Geochemistry》2004,19(5):645-664
Sediment and water samples from 12 saline pans on the semi-arid west coast of South Africa were analysed to determine the origin of salts and geochemical evolution of water in the pans. Pans in the area can be subdivided into large, gypsiferous coastal pans with 79–150 g/kg total dissolved salt (TDS), small inland brackish to saline (2–64 g/kg TDS) pans and small inland brine (168-531 g/kg TDS) pans that have a layer of black sulphidic mud below a halite crust. The salinity of coastal pan waters varies with the seasonal influx of dilute runoff and dissolution of relict Pleistocene marine evaporite deposits. In contrast, inland pans are local topographic depressions, bordered on the north by downslope lunette dunes, where solutes are concentrated by evaporation of runoff, throughflow and groundwater seepage. The composition of runoff and seepage inflow waters is determined by modification of coastal rainfall by weathering, calcite precipitation and ion exchange reactions in the predominantly granitic catchment soils. Evaporation of pan waters leads to precipitation of calcite, Mg–calcite, dolomite, gypsum and halite in a distinct stratigraphic succession in pan sediments. Bicarbonate limits carbonate precipitation, Ca limits gypsum precipitation and Na limits halite precipitation. Dolomitisation of calcite is enhanced by the high Mg/Ca ratio of brine pan waters. Brine pan waters evolve seasonally from Na–Cl dominated brines in the wet winter months to Mg–Cl dominated brines in the dry summer months, when 5–20 cm thick halite crusts cover pan surfaces. Pan formation was probably initiated during a drier climate period in the early Holocene. More recent replacement of natural vegetation by cultivated land may have accelerated salt accumulation in the pans. 相似文献
2.
The origin and evolution of formation water from Upper Jurassic to Upper Cretaceous mudstone–packstone–dolomite host rocks at the Jujo–Tecominoacán oil reservoir, located onshore in SE-Mexico at a depth from 5200 to 6200 m.b.s.l., have been investigated, using detailed water geochemistry from 12 producer wells and six closed wells, and related host rock mineralogy. Saline waters of Cl–Na type with total dissolved solids from 10 to 23 g/L are chemically distinct from hypersaline Cl–Ca–Na and Cl–Na–Ca type waters with TDS between 181 and 385 g/L. Bromine/Cl and Br/Na ratios suggest the subaerial evaporation of seawater beyond halite precipitation to explain the extreme hypersaline components, while less saline samples were formed by mixing of high salinity end members with surface-derived, low salinity water components. The dissolution of evaporites from adjacent salt domes has little impact on present formation water composition. Geochemical simulations with Harvie-Mφller-Weare and PHRQPITZ thermodynamic data sets suggest secondary fluid enrichment in Ca, HCO3 and Sr by water–rock interaction. The volumetric mass balance between Ca enrichment and Mg depletion confirms dolomitization as the major alteration process. Potassium/Cl ratios below evaporation trajectory are attributed to minor precipitation of K feldspar and illitization without evidence for albitization at the Jujo–Tecominoacán reservoir. The abundance of secondary dolomite, illite and pyrite in drilling cores from reservoir host rock reconfirms the observed water–rock exchange processes. Sulfate concentrations are controlled by anhydrite solubility as indicated by positive SI-values, although anhydrite deposition is limited throughout the lithological reservoir column. The chemical variety of produced water at the Jujo–Tecominoacán oil field is related to a sequence of primary and secondary processes, including infiltration of evaporated seawater and original meteoric fluids, the subsequent mixing of different water types and the formation of secondary minerals by water–rock interaction. A best fit between measured and calculated reservoir temperatures was obtained with the Mg–Li geothermometer for high salinity formation water (TDS > 180 g/L), whereas Na–K, Na–Ka–Ca and quartz geothermometers are partially applicable for less salinite water (TDS < 23 g/L). 相似文献
3.
根据岩石薄片、Ｘ衍射和扫描电镜分析资料,本文研究了巴州坳陷下白垩统—中侏罗统粘土矿物特征,发现粘土矿物分为伊利石、伊／蒙混层和绿泥石三种类型。粘土矿物的类型和含量随深度而变化,形成了伊／蒙混层带、混层迅速转化带和伊利石带。粘土矿物的转化和自生粘土矿物的形成是沉积地层非常重要的成岩变化。 相似文献
4.
CAI Chunfang PENG Licai MEI Bowen XIAO Yingkai 《《地质学报》英文版》2006,80(4):550-556
In order to elucidate the origin and migration of basinal brines in the Bachu Bulge, Tarim Basin, we have carried out analyses on chemical composition, and boron, hydrogen and oxygen isotopes of formation waters together with the XRD of clay minerals from the Paleozoic strata. The waters show Ca, B, Li and Sr enrichment and SO4 depletion in the Carboniferous and Ordovician and K enrichment in part of the Ordovician relative to seawater. The relationship between δD and δ^18O shows that all the data of the waters decline towards the Global Meteoric Water Line with the intersection of them close to the present-day local meteoric water, suggesting that modern meteoric water has mixed with evaporated seawater. The ^87Sr/^86Sr ratios range from 0.7090 to 0.7011, significantly higher than those of the contemporary seawater. The δ^11B values range from ＋19.7 to ＋32.3‰, showing a decrease with the depth and B concentrations. The results suggest that isotopically distinct B and Sr were derived from external sources. However, since the percentages of illite are shown to increase with depth among clay minerals in the study area, i.e., illite is due to precipitation rather than leaching during deeper burial, it is unlikely for illite to have contributed a significant amount of B to the waters. Thus, B with low δ^11B values is interpreted to have been added mainly from thermal degradation of kerogen or the basalts in the Cambrian and Lower Ordovician. 相似文献
5.
N.V. Guseva Yu.G. Kopylova Ch.K. Oidup K.D. Arakchaa K.M. Rychkova A.A. Khvashchevskaya O.D. Ayunova 《Russian Geology and Geophysics》2018,59(2):135-143
Groundwater with high salinity is widespread in different climatic and geologic environments of the world. The formation of its chemical composition, however, is still debatable. The chemical composition of groundwater has been studied in 19 springs of the Tuva depression. In this area, hydrocarbonate, sulfate, and chloride waters with different cation compositions discharge. Their TDS value varies mainly from 1 to 6 g/L, reaching 315 g/L at only one locality. The chemical composition of the studied waters is reflective of the geostructural, hydrogeologic, landscape, and geochemical conditions. The main processes determining the chemical composition of the waters are their interaction with aluminosilicate minerals, dissolution of gypsum and halite, evaporation, and oxidation of sulfide minerals. 相似文献
6.
Murdmaa I. O. Bogdanova O. Yu. Gorshkov A. I. Novikov G. V. Shevchenko V. P. 《Lithology and Mineral Resources》2000,35(6):594-597
The mineralogy of suspended matter from surface and bottom waters is studied at two sites in the Barents Sea. Along with terrigenous minerals, the suspended matter samples contain authigenic mineral phases of iron and manganese oxyhydroxides. Mn-feroxyhite, Fe-vernadite, goethite, and proto-ferrihydrite were identified in samples from surface waters, whereas birnessite and nonferruginous vernadite were registered in samples from bottom waters. The formation of suspended manganese minerals in bottom waters is explained by an additional Mn supply from underlying reduced sediments during their early diagenesis and oxygen depletion in the near-bottom nepheloid layer. Bacteria are supposed to take part in the authigenic mineral formation. 相似文献
7.
人工回灌过程中所发生的水-岩相互作用是影响回灌层位地下水环境质量的重要因素。采用室内实验和水文地球化学模拟等技术对人工回灌过程中的水-岩相互作用机理进行了分析。研究结果表明：受混合作用影响,随着回灌水比例的增加,混合水中TDS质量浓度降低,水化学类型由Cl·HCO3-Na型水逐渐转变为HCO3·Cl-Na·Ca型水;受水-岩作用影响,在同一混合比例条件下,随着水-岩作用的进行,混合水中TDS质量浓度升高,各主要离子质量浓度呈现升高的趋势,但只有回灌水比例占10%时,混合水TDS质量浓度才大于原始地下水（涨幅约5%）。实验介质溶解于水的离子中,Ca2+、Mg2+和HCO-3主要来源于碳酸盐矿物的溶解, Na+主要来自岩盐的溶解。在人工回灌过程中,发生的水-岩相互作用主要包括方解石、白云石、钾长石、岩盐、CO2的溶解和伊利石的沉淀。其中:钾长石溶解量与伊利石沉淀量、碳酸盐矿物溶解量与CO2溶解量的相关性较强,其相关系数分别为1.00和0.78（显著性水平为0.05）;硅酸盐矿物反应量和回灌水比例之间的相关系数为0.97（显著性水平为0.01）,相关性极强;而碳酸盐矿物反应量和回灌水比例之间的相关系数为0.52（显著性水平为0.01）,相关性较弱。上述相关性分析为确定人工回灌过程中的水-岩相互作用机理、地下水中主要离子组分的来源途径以及定量分析人工回灌对含水层介质的影响提供了依据。 相似文献
8.
柴达木西部南翼山构造地表混积岩岩石学特征及沉积环境讨论 总被引：1，自引：0，他引：1
南翼山构造地表狮子沟组发育混积岩,作为一种特殊类型的沉积岩,其研究具有一定的实际意义和科学价值。本文在野外观察和镜下鉴定的基础上,对南翼山混积岩样品进行了X衍射、主微量元素及碳氧同位素测试,分析了混积岩的岩石学特征,考虑到其成分和成因的复杂性,通过数据分析排除了多种干扰因素,最后利用有效指标综合判断了其沉积环境。结果显示：南翼山构造地表混积岩中陆源碎屑平均含量为58.7%,碳酸盐矿物含量为31.0%,属于碳酸盐质陆源碎屑岩,主要为钙质泥岩,其中碎屑矿物以细粉砂级石英为主,碳酸盐矿物主要为泥晶方解石,黏土矿物组合为伊利石和有序伊蒙混层,且三者呈均匀混合的特征。数据分析表明Ca、Na、Mn、Sr、Ba等元素主要来源于自生矿物,稀土元素及碳氧同位素组成未受成岩作用影响,可以作为判断沉积时水体盐度和氧化还原条件的指标。根据Sr/Cu比值和K2 O/Al 2O3比值,结合黏土矿物组合及伊利石结晶度和化学指数,判断地表混积岩沉积时为寒冷干旱的气候条件;Sr/Ba比值和Z值表明古水体介质为咸水环境;U/Th比值、自生U含量和Ce轻微负异常等指标综合判定其形成于弱氧化环境。以上研究表明,南翼山构造地表混积岩主要为陆源碎屑和碳酸盐矿物均匀混合的钙质泥岩,形成于寒冷干旱气候条件下的弱氧化咸水湖泊环境中。 相似文献
9.
《Applied Geochemistry》2004,19(9):1355-1365
Hydrogeochemical assessment of 40 saline waters and brines from 20 locations within the lower (southern) and middle regions of the Benue-Trough, Nigeria are presented and discussed in terms of genesis of the primary salinity and subsequent hydrochemical evolution. The total dissolved ions range from 5263 to 88,800 mg/L and 5148 to 47,145 mg/L in the lower and middle region, respectively.The saline waters and brines are characteristically Na–Cl type enriched in Ca and Sr on the one hand and depleted in Mg and SO4 on the other, relative to the seawater evaporation trend. Ionic ratios, Na–Cl–Br systematic and divalent cations suggest two likely sources of primary salinity: a fossil seawater source and dissolution of halite. However, water–rock interaction involving Mg uptake by clay minerals and possibly dolomitization during diagenesis appear to be responsible for further modification of the primary chemistry. A conceptualized hydrogeological/flow model for the brines is presented. 相似文献
10.
The Upper Red Formation (URF) comprises over 1–5 km of late Miocene siliciclastic sediments in the Central Iran Basin. The formation is dominated by volcaniclastic conglomerates and arenites. The prevailing arid conditions during most of the basin's history resulted in deposition of predominantly organic‐poor, red sediments with gypsum and zeolites. This investigation concentrates on the mineralogy and geochemistry of the URF in the southern and northern margins of the basin where the formation was buried to depths of 2.4 and 6.6 km, respectively. Fine fraction mineral separates from the southern margin consist of nearly pure smectite and zeolites at a depth of 400 m and smectite with minor quartz and calcite at 1800 m. Shallow samples (1350 m) from the northern section are rich in smectite, illite/smectite with some discrete illite and chlorite. This assemblage is progressively replaced by discrete illite and chlorite with increasing burial depth so that only these two minerals are found at depths greater than 4300 m. The initial alteration process involved replacement of glass and volcanic lithics by smectite and zeolites in both margins of the basin. Increased depth of burial in the northern margin resulted in the progressive isochemical alteration of smectite to discrete illite and chlorite. Diagenesis of clay assemblages occurred essentially in a closed system. Solute products of glass hydrolysis reactions were retained in highly alkaline, saline ground waters from which zeolites, carbonates and oxides precipitated as cements. It is unlikely that these sediments were ever significantly leached by meteoric waters or by organic acids generated during burial diagenesis. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
11.
12.
H. Ferchichi M. F. Ben Hamouda B. Farhat A. Ben Mammou 《International Journal of Environmental Science and Technology》2018,15(11):2473-2492
The integration of the statistical approaches and GIS tools with the hydrogeological and geological contexts allowed the assessment of the processes that cause groundwater quality deterioration in the great important deltaic aquifer in the northeastern Tunisia (Medjerda Lower Valley Aquifer). The spatial variation of the groundwater parameters and the molar ratio (Cl?/Br?) were also used to determine the possible impacts from seawater intrusion and from the septic tank leachate. Sixty shallow groundwater samples were collected in 2014 and analyzed for major and trace ions over an area of about 1090 km2 to determine the suitability for drinking or agricultural purposes. The total dissolved solids (TDS) content ranges from 1005 to 19,254 mgl?1 with a mean value of 3477.18 mgl?1. The chemistry is dominated by the sodium–chloride waters (55%). Mapping of TDS, Cl?, Na+, SO42? and NO3? using kriging method shows a clear increase in salinity toward the coastline accompanied by Na+ and Cl? increase which may be related to seawater intrusion and halite dissolution. Locally, higher nitrate concentration is related to the agricultural activities inducing contribution of chemical fertilizers and irrigation with treated wastewater. The saturation indices indicate that all carbonate minerals tend to reach saturation equilibrium confirming water–rock interactions, while evaporitic minerals are still in sub-saturation state and may increase the salinity of the groundwater. The principal component analysis proves the occurrence of groundwater contamination principally by seawater intrusion in the factor I (74.15%) and secondary by an anthropogenic source in the factor II (10.35%). 相似文献
13.
Hermann Harder 《Chemical Geology》1974,14(4):241-253
The synthesis of illite mixed-layer minerals at surface conditions is possible through precipitation of Al hydroxides from Si-, Mg- and K-containing solutions. It has been shown that amorphous hydroxides of Al, Fe, etc. are capable of coprecipitating silica even from very dilute solutions. By aging of these X-ray amorphous hydroxide—silica precipitates under certain conditions, clay minerals can be synthesized at low temperatures. The presence of Mg particularly favors the formation of three-layer clay minerals. Mg-rich Al hydroxide—silica precipitates permit formation of tri- and di-octahedral smectite, illite and chlorite. The formation of three-layer clay minerals is only possible when the precipitates contain at least 6% MgO. The precipitates stay amorphous if the Mg content is lower. The adsorption of Mg and K on the hydroxide—silica precipitate controls the illite or montmorillonite portion in the mixture of the three-layer silicates. There is a competition for K and Mg adsorption on the hydroxide—silica precipitates. Higher K concentration inhibits the three-layer mineral formation through the lowering of the Mg content in the precipitates. Illite mineral formation is favored under certain K/Mg ratios. Higher NaCl contents do not favor the three-layer mineral formation.The enrichment of Mg and K in the precipitates is not as large as the enrichment of Si in the hydroxides. This means that the illite mineral formation is only possible from solutions with a high-salt content like seawater. 相似文献
14.
探讨了渤中坳陷石臼陀凸起东段CO2来源及CO2充注对储层粘土矿物的影响.研究表明,CO2中δ13C组成较重,R/Ra值较大,CO2为幔源成因;控盆的深大断裂是CO2的主要运移通道;CO2热流体晚期充注对砂岩储集层粘土矿物产生了明显的影响:CO2热流体侵位后形成的热波动效应加快了储集层中伊蒙混层粘土的演化,含CO2储集层中伊蒙混层中蒙脱石含量要比同深度的泥岩低15％ ～30％;CO2热流体晚期侵入加剧了长石的溶蚀作用,长石溶蚀促进了自生高岭石的大量形成;CO2热流体侵位后形成的偏酸性环境抑制伊利石生长,促进了其他粘土矿物向高岭石转化;含CO2储集层以少见的高自生高岭石、低伊利石为特征,这对储层物性改善起到了决定性的影响. 相似文献
15.
Halil Murat Özler 《Environmental Earth Sciences》2010,61(2):323-340
There are 59 springs at the Gevas–Gurp?nar–Güzelsu basins, 38 of these springs emerge from the fractured karst aquifers (recrystallized limestone and travertine) and 21 emerge from the Yuksekova ophiolites, K?rkgeçit formation and alluvium. The groundwater samples collected from 38 out of the total of 59 springs, two streams, one lake and 12 wells were analyzed physico-chemically in the year 2002. EC and TDS values of groundwater increased from the marble (high altitude) to the ophiolites and alluvium (toward Lake Van) as a result of carbonate dissolution and connate seawater. Five chemical types of groundwater are identified: Ca–Mg–HCO3, Mg–Ca–HCO3, Mg–Na–HCO3, Na–Ca–HCO3 and Mg–Ca–Na–HCO3. The calculations and hydrochemical interpretations show that the high concentrations of Ca2+, Mg2+ and HCO3 ? as predominant ions in the waters are mainly attributed to carbonate rocks and high pCO2 in soil. Most of the karst springs are oversaturated in calcite, aragonite and dolomite and undersaturated in gypsum, halite and anhydrite. The water–rock interaction processes that singly or in combination influence the chemical composition of each water type include dissolution of carbonate (calcite and dolomite), calcite precipitation, cation exchange and freshening of connate seawater. These processes contribute considerably to the concentration of major ions in the groundwater. Stable isotope contents of the groundwater suggest mainly direct integrative recharge. 相似文献
16.
Hydrochemistry of groundwater and its assessment for irrigation purpose in coastal Jeffara Aquifer, southeastern Tunisia 总被引：1，自引：0，他引：1
Groundwater is of a paramount importance in arid areas, as it represents the main water resource to satisfy the different needs of the various sectors. Nevertheless, coastal aquifers are generally subjected to seawater intrusion and groundwater quality degradation. In this study, the groundwater quality of the coastal Jeffara aquifer (southeastern Tunisia) is evaluated to check its suitability for irrigation purposes. A total of 74 groundwater samples were collected and analyzed for various physical and chemical parameters, such as, electrical conductivity, pH, dissolved solids (TDS), Na, K, Ca, Mg, Cl, HCO3, and SO4. Sodium adsorption ratio, magnesium adsorption ratio, Sodium percentage, and permeability index were calculated based on the analytical results. The analytical results obtained show a strong mineralization of the water in the studied aquifer. TDS concentrations range from 3.40 to 18.84 g?L?1. Groundwater salinity was shown to be mainly controlled by sodium and chloride. The dominant hydrochemical facieses are Na–Cl–Ca–SO4, mainly as a result of mineral dissolution (halite and gypsum), infiltration of saline surface water, and seawater intrusion. Assessment of the groundwater quality of the different samples by various methods indicated that only 7% of the water, in the northwest of the study area, is considered suitable for irrigation purposes while 93% are characterized by fair to poor quality, and are therefore just suitable or unsuitable for irrigation purposes. 相似文献
17.
Boutheina Farhat Abdallah Ben Mammou Lamia Kouzana Ismail Chenini Francesca Podda Giovanni De Giudici 《Resource Geology》2010,60(4):377-388
The present paper investigates hydrochemical processes and water quality in the Mornag aquifer in NE Tunisia. Groundwater samples were collected during a field campaign, and were analysed for major and trace elements. The collected waters have a chemical facies rich in Ca2+, Na+ and Cl-. Piper diagram shows a progressive increase in chloride ions along with increasing salinity. Saturation indexes calculated by using PHREEQC (USGS) show that the Mornag waters are slightly saturated with respect to carbonates (calcite and dolomite), while undersaturated with respect to gypsum, halite and other evaporitic minerals. The current composition of waters takes place via dissolution of halite and Ca-sulfates, where the increase in calcium is partially balanced by possible calcite precipitation. The relevant recorded pollutant is nitrate, which was likely dispersed from agricultural soils, while heavy metals were generally far below values of pollution thresholds, indicating no influence by mining activity. 相似文献
18.
新疆巴里坤盐湖是一个常年性固、液并存的硫酸盐型盐湖。盐湖卤水中含Ｎａ＋、Ｋ＋、Ｃａ２＋、Ｃｌ－、ＳＯ２－４、ＨＣＯ－３、ＣＯ２－３等主要成分，沉积物中有芒硝、无水芒硝、石膏、水钙芒硝、半水石膏、石盐等盐类矿物及碳酸盐和泥质矿物。盐湖中有大量卤虫及卤虫卵自湖中心向湖岸呈环带状分布，在成盐过程中起着重要作用。盐湖形成于第三纪，第四纪以来，曾经历２次成岩期，约自１７ｋａＢ．Ｐ．湖水多次蒸发浓缩，成岩作用加强，形成芒硝等矿产 相似文献
19.
Samir Mefteh Mounir Medhioub Elhoucine Essefi Fakher Jamoussi 《Journal of the Geological Society of India》2014,83(2):198-210
This study aims to follow the effect of the diagenetic transformations on the clayey fraction and the organic matter of the Tunisian southern sub-surface. 61 samples from oil well named NWA-1 were recuperated for series of analyses. This study follows a comparative approach between the mineralogical, geochemical and petrographic studies. To discuss results from a statistical viewpoint, the Principal Component Analysis (PCA) was applied in order to find out any correlation between different components. The associated minerals quartz, feldspar, calcite, pyrite, anhydrite, gypsum, dolomite and olivine are also detected. These associated minerals remove by-products by the illitization reaction. The Index of Crystallinity (IC) of illite shows that, except some anomalies, the studied samples are between the epizone and the anchizone. Downward, samples show the effect of diagenetic processes and weak signs of low-grade metamorphism. As regards to the organic matter, values of Tmax range between 333°C and 463°C. On the other hand, potential hydrocarbon compounds (S2) show low values compared to those of (S1); but they maintain a similar variability from 0.63 to 21.12. SEM observations and X-ray microanalyses supported the formation of authigenic micro-quartz. The PCA of clay minerals, chemical components, and the depth shows three different populations. Feldspar, chlorite and quartz make up a population positively correlated with the depth. The second population seems to be indifferent to depth variation; it is made up of two sub-populations: the population of illite, gypsum and anhydrite, which is obtained by a counter clock rotation of depth population; and the population of pyrite, kaolinite, olivine phyllosilicate, which is obtained by an anticlockwise rotation of depth population. Third, the population of smectite, calcite and dolomite is inversely proportional to the depth variation. On the other hand, the PCA of TOC, Tmax, HI, S1, S2 and the depth make up a homogenous statistical population following the depth evolution. 相似文献
20.
G. S. Pundeer 《Contributions to Mineralogy and Petrology》1969,23(1):65-85
20 core samples from the dolomite-anhydrite sequence overlying the Werra-anhydrites (Zechstein 1) were examined. The formation consists of brecciated shaly clay in a groundmass of dolomite and anhydrite with small amounts of rocksalt. The drillhole is located near the village Bruennighausen (N. Germany) on the south west flank of a saltdome.Chlorites and illite are the only clay minerals present. Chlorites: three different varieties could be distinguished, predominate in the upper portion whereas the content of illite increases in the lower part. A regeneration of illite in the upper part of the profile has been found by comparison of the K2O-content of the illite (9–10%=upper part, 8%=lower part). Diagenetic formation of quartz and feldspars was also observed throughout the profile. The ratio of authigenic quartz/detrital quartz deoreasss in lower part. At least two generations of dolomite have been found and also pseudomorphs of dolomite after gypsum.The investigations have shown, that the shaly clay was deposited in a saline environment. Diagenetic changes after deposition were due to increasing salinity of the pore solution of the sediment. Brecciation took place long after compaction of the clay. It was accompanied and followed by further diagenetic changes. 相似文献